S-1-Boc-3-pyrrolidinecarboxylic acid

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Reagent Code: #234235
label
Alias (S)-1-Boc-pyrrolidine-3-carboxylic acid
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CAS Number 140148-70-5

science Other reagents with same CAS 140148-70-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.25 g/mol
Formula C₁₀H₁₇NO₄
badge Registry Numbers
MDL Number MFCD03094728
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected amine and carboxylic acid functionalities make it ideal for peptide coupling and heterocycle formation. Commonly employed in the preparation of pyrrolidine-based drugs, including those targeting central nervous system disorders and protease inhibitors. The Boc group allows for selective deprotection under mild acidic conditions, enabling stepwise assembly in complex molecule synthesis. Widely utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and ability to mimic proline-like structures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿159.50
inventory 1g
10-20 days ฿517.00
inventory 5g
10-20 days ฿1,815.00

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S-1-Boc-3-pyrrolidinecarboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected amine and carboxylic acid functionalities make it ideal for peptide coupling and heterocycle formation. Commonly employed in the preparation of pyrrolidine-based drugs, including those targeting central nervous system disorders and protease inhibitors. The Boc group allows for selective deprotection under mild acid

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its protected amine and carboxylic acid functionalities make it ideal for peptide coupling and heterocycle formation. Commonly employed in the preparation of pyrrolidine-based drugs, including those targeting central nervous system disorders and protease inhibitors. The Boc group allows for selective deprotection under mild acidic conditions, enabling stepwise assembly in complex molecule synthesis. Widely utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and ability to mimic proline-like structures.

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